Walter F. Hink

Replication and infectivity of the nuclear polyhedrosis virus of the alfalfa looper, Autographa californica, produced in cells grown in vitro

Abstract A virus isolated from the alfalfa looper, Autographa californica, replicated successfully and rapidly in a suspended ovarian cell line of the cabbage looper, Trichoplusia ni. Polyhedra were observed in the nucleus of cells within 20 hr after inoculation. The cytopathological changes typical of nuclear polyhedrosis infections were observed, and an average of 64 polyhedra/cell were produced. These polyhedra were quantitatively as infectious to cabbage looper larvae as those produced in vivo. In addition, they were infective to Heliothis virescens, Pectinophora gossypiella, Spodoptera exigua, A. californica, and Anagrapha falcifera.

Replication and serial passage of infectious Heliothis nucleopolyhedrosis virus in an established line of Heliothis zea cells

Abstract An established cell line derived from the ovary of adults of the cotton bollworm, Heliothis zea, supported growth of the Heliothis nucleopolyhedrosis virus (NPV). Typical NPV symptoms were obtained when infected cells were fed to neonatal bollworms; however, the cell line never produced free virions or inclusion bodies containing virions. Infectious virus was passed through the cell line 7 consecutive times, using only infected cells from the previous pass. Infectivity at the 7th serial-pass represented a dilution of >10−8 of the original inoculum.

Infection of synchronized TN-368 cell cultures with alfalfa looper nuclear polyhedrosis virus

Abstract Synchronized cultures of the TN-368 insect cell line were infected with a nuclear polyhedrosis virus from the alfalfa looper, Autographa californica , during different phases of the cell cycle. Cultures exposed to virus during the middle and late S phase have higher percentages of infected cells than cultures inoculated with virus in the G 2 phase. The amount of virus produced from each infected cell (polyhedra and plaque forming units) is not significantly different between cultures infected at all phases of the cell cycle.

Comparison of nuclear polyhedrosis virus replication in five lepidopteran cell lines.

Abstract Comparative studies were performed on the replication of the Autographa californica nuclear polyhedrosis virus in cell lines from Estigmene acrea, BTI-EAA; Lymantria dispar, IPLB-LD64BA; Mamestra brassicae, IZD-MB0503; Spodoptera frugiperda, IPLB-SF1254; and Trichoplusia ni, TN-368. Significant differences were observed in the amount of virus obtained from the cell lines, with M. brassicae and T. ni producing more polyhedra than the other lines. These two cell lines also produced nonoccluded virus most rapidly, followed by S. frugiperda, E. acrea, and L. dispar. Sensitivities of the cell lines to infection by the virus, as determined by plaque formation, followed the same pattern, with M. brassicae being most sensitive and L. dispar least so. The T. ni cell line produced polyhedra which were more pathogenic to T. ni larvae than those from the other cells. These differences have important implications in the application of cell cultures in the development of microbial insecticides.

Comparative sensitivity of several plaque assay techniques employing TN-368 and IPLB-SF 21AE insect cell lines for plaque variants of Galleria mellonella nuclear polyhedrosis virus

Abstract Several plaque assay techniques employing TN-368 or IPLB-SF 21AE cells were evaluated for their usefulness in detecting and distinguishing MP (many polyhedra) and FP (few polyhedra) plaque variants of Galleria mellonella nuclear polyhedrosis virus. Both plaque morphologies were produced using either cell line. Of the overlays tested, the buffered 0.6% methylcellulose overlay yielded the most plaques and was best suited for titration. It was also the easiest overlay to prepare and use. The largest plaques were obtained using either cell line with the 1.0 or 0.75% agarose overlays. Plaque variants were most easily distinguished under 1.0 or 0.75% agarose overlays with IPLB-SF 21 cells. The 0.9% MC overlay was the only overlay which did not allow detection of FP plaques. However, FP plaques were detected using a buffered modification of this overlay. It is concluded that the FP variant of G. mellonella NPV is not a host-dependent phenomenon, and that its detection can be influenced by overlay formulation.

Selection of Autographa californica nuclear polyhedrosis virus for resistance to inactivation by near ultraviolet, far ultraviolet, and thermal radiation

Abstract Experiments were performed to isolate strains of Autographa californica nuclear polyhedrosis virus (Baculovirus) with inherent resistance to inactivation by far ultraviolet radiation, near ultraviolet radiation, and thermal radiation. Virus with apparently increased resistance to inactivation by near ultraviolet radiation was isolated. Virus with increased resistance to far ultraviolet radiation was not obtained. No significant differences in response to thermal radiation were observed between wild virus and virus selected for increased resistance to inactivation by this agent. Repeated selection treatment with far ultraviolet radiation and with near ultraviolet radiation resulted in the production of virus with significantly reduced virulence in comparison with wild virus. The virulence of heat-selected virus did not differ from wild virus.